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COMT c.109_110delinsCT ;(p.G37L)
Variant ID: 22-19950158-GG-CT
NM_000754.3(
COMT
):c.109_110delinsCT;(p.G37L)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Insights into the Molecular Mechanisms of Alzheimer's and Parkinson's Diseases with Molecular Simulations: Understanding the Roles of Artificial and Pathological Missense Mutations in Intrinsically Disordered Proteins Related to Pathology.
International Journal Of Molecular Sciences
Coskuner-Weber, Orkid O; Uversky, Vladimir N VN
Publication Date: 2018-01-24
Variant appearance in text: COMT: G37L
PubMed Link:
29364151
Variant Present in the following documents:
Main text
View BVdb publication page